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安宫牛黄丸对大鼠脑缺血诱导的细胞凋亡具有保护作用:上调Bcl-2并下调Bax和caspase-3。

An-Gong-Niu-Huang Wan protects against cerebral ischemia induced apoptosis in rats: up-regulation of Bcl-2 and down-regulation of Bax and caspase-3.

作者信息

Wang Guo-Hua, Lan Rui, Zhen Xin-De, Zhang Wen, Xiang Jun, Cai Ding-Fang

机构信息

Department of Integrative Medicine, Zhongshan Hospital, and Laboratory of Neurology, Institute of Integrative Medicine, Fudan University, Shanghai 200032, China.

Department of Radiology, Zhongshan Hospital, Fudan University, Shanghai 200032, China.

出版信息

J Ethnopharmacol. 2014 May 28;154(1):156-62. doi: 10.1016/j.jep.2014.03.057. Epub 2014 Mar 29.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

The An-Gong-Niu-Huang Wan (AGNH), a Chinese traditional medicine, has been used for treatment of cerebral diseases for centuries in China and other Asian countries, and is approved by the State Food and Drug Administration of China for the treatment of stroke. The aim of present study is to test the neuroprotective effects of AGNH on cerebral ischemia in rats and to explore the underlying mechanisms.

MATERIALS AND METHODS

75 Male Sprague-Dawley rats were randomly divided into 5 groups: sham, ischemia-reperfusion (I/R), and I/R plus 0.065 g/kg/d AGNH, 0.125 g/kg/d AGNH and 0.25 g/kg/d AGNH. Cerebral ischemia was induced by 1.5h of middle cerebral artery occlusion (MCAO). Neurological functional deficits were evaluated according to Zea longa׳s score, cerebral infarct area was measured by tetrazolium staining. Cell injury and apoptosis were assessed by Nissl staining and DNA fragmentation assay. The expression of Bax, Bcl-2 and caspase-3 were analyzed by Western blot.

RESULTS

Rats subjected to MCAO exhibited worsened neurological score, infarct area, cell damage and apoptosis. These were all attenuated by AGNH (0.125 and 0.25 g/kg/d). Moreover, AGNH reversed cerebral ischemia induced decreases in Bcl-2 expression and increases in Bax and caspase-3 expression.

CONCLUSIONS

These results suggest that AGNH exerts neuroprotective effects, and the neuroprotection is likely to relate to depressed Bax/Bcl-2 ratio and caspase-3 level, leading to inhibition of apoptotic cell death.

摘要

民族药理学相关性

安宫牛黄丸(AGNH)是一种中药,在中国和其他亚洲国家已被用于治疗脑部疾病数百年,并被中国国家食品药品监督管理总局批准用于治疗中风。本研究的目的是测试AGNH对大鼠脑缺血的神经保护作用,并探讨其潜在机制。

材料与方法

75只雄性Sprague-Dawley大鼠随机分为5组:假手术组、缺血再灌注(I/R)组、I/R + 0.065 g/kg/d AGNH组、I/R + 0.125 g/kg/d AGNH组和I/R + 0.25 g/kg/d AGNH组。通过大脑中动脉闭塞(MCAO)1.5小时诱导脑缺血。根据Zea longa评分评估神经功能缺损,通过四氮唑染色测量脑梗死面积。通过尼氏染色和DNA片段化分析评估细胞损伤和凋亡。通过蛋白质免疫印迹法分析Bax、Bcl-2和caspase-3的表达。

结果

接受MCAO的大鼠神经评分、梗死面积、细胞损伤和凋亡均恶化。这些均被AGNH(0.125和0.25 g/kg/d)减轻。此外,AGNH逆转了脑缺血诱导的Bcl-2表达降低以及Bax和caspase-3表达增加。

结论

这些结果表明AGNH具有神经保护作用,并且这种神经保护作用可能与降低Bax/Bcl-2比值和caspase-3水平有关,从而导致对凋亡性细胞死亡的抑制。

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